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Pregnancy-associated progenitor cells: an under-recognized potential source of stem cells in maternal lung.妊娠相关祖细胞:母体肺中干细胞的潜在未被认识来源。
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Transfer and Integration of Breast Milk Stem Cells to the Brain of Suckling Pups.母乳干细胞向哺乳期幼仔大脑的转移和整合。
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PLoS One. 2015 May 6;10(5):e0124747. doi: 10.1371/journal.pone.0124747. eCollection 2015.
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Cell fusion in the brain: two cells forward, one cell back.大脑中的细胞融合:前进两步,后退一步。
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HLA-targeted cell sorting of microchimeric cells opens the way to phenotypical and functional characterization.微嵌合细胞的HLA靶向细胞分选为表型和功能特征分析开辟了道路。
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本文引用的文献

1
Pregnancy-associated progenitor cells differentiate and mature into neurons in the maternal brain.妊娠相关祖细胞在母体大脑中分化并成熟为神经元。
Stem Cells Dev. 2010 Dec;19(12):1819-30. doi: 10.1089/scd.2010.0046. Epub 2010 Sep 13.
2
Increased fetal cell trafficking in murine lung following complete pregnancy loss from exposure to lipopolysaccharide.脂多糖暴露导致完全妊娠丢失后,胎鼠肺部胎细胞迁移增加。
Fertil Steril. 2010 Mar 15;93(5):1718-1721.e2. doi: 10.1016/j.fertnstert.2009.08.042. Epub 2009 Oct 7.
3
Fetal microchimeric cells participate in tumour angiogenesis in melanomas occurring during pregnancy.胎儿微嵌合细胞参与孕期发生的黑色素瘤的肿瘤血管生成。
Am J Pathol. 2009 Feb;174(2):630-7. doi: 10.2353/ajpath.2009.080566. Epub 2009 Jan 15.
4
Increased fetal cell microchimerism in high grade breast carcinomas occurring during pregnancy.孕期发生的高级别乳腺癌中胎儿细胞微嵌合体增加。
Int J Cancer. 2009 Mar 1;124(5):1054-9. doi: 10.1002/ijc.24036.
5
Early phase of maternal skin carcinogenesis recruits long-term engrafted fetal cells.
Int J Cancer. 2008 Dec 1;123(11):2512-7. doi: 10.1002/ijc.23819.
6
Breast cancer stroma frequently recruits fetal derived cells during pregnancy.乳腺癌基质在孕期常募集源自胎儿的细胞。
Breast Cancer Res. 2008;10(1):R14. doi: 10.1186/bcr1860. Epub 2008 Feb 13.
7
Pregnancy allows the transfer and differentiation of fetal lymphoid progenitors into functional T and B cells in mothers.怀孕可使胎儿淋巴细胞祖细胞转移并分化为母亲体内具有功能的T细胞和B细胞。
J Immunol. 2008 Jan 15;180(2):889-97. doi: 10.4049/jimmunol.180.2.889.
8
Maternal neoangiogenesis during pregnancy partly derives from fetal endothelial progenitor cells.孕期母体的新生血管形成部分源自胎儿内皮祖细胞。
Proc Natl Acad Sci U S A. 2007 Feb 6;104(6):1871-6. doi: 10.1073/pnas.0606490104. Epub 2007 Jan 31.
9
Robert E. Gross Lecture. Fetomaternal cell trafficking: a story that begins with prenatal diagnosis and may end with stem cell therapy.罗伯特·E·格罗斯讲座。母胎细胞转运:一个始于产前诊断且可能以干细胞治疗告终的故事。
J Pediatr Surg. 2007 Jan;42(1):12-8. doi: 10.1016/j.jpedsurg.2006.09.047.
10
Fetal cells participate over time in the response to specific types of murine maternal hepatic injury.随着时间的推移,胎儿细胞参与对特定类型的小鼠母体肝脏损伤的反应。
Hum Reprod. 2007 Mar;22(3):654-61. doi: 10.1093/humrep/del426. Epub 2006 Oct 30.

母胎微嵌合体:一些答案与诸多新问题。

Fetomaternal microchimerism: Some answers and many new questions.

作者信息

Tan Kian Hwa, Zeng Xiao Xia, Sasajala Piriya, Yeo Ailing, Udolph Gerald

机构信息

Institute of Medical Biology; Singapore.

出版信息

Chimerism. 2011 Jan;2(1):16-8. doi: 10.4161/chim.2.1.14692.

DOI:10.4161/chim.2.1.14692
PMID:21547031
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3084951/
Abstract

The transfer of fetal cells into mothers during pregnancy and their organ specific integration is a well recognized phenomenon in placental vertebrates. Recently, it has been reported that some fetal cells found in the mothers have progenitor cell-like features such as multilineage differentiation potential and as a consequence they were termed pregnancy associated progenitor cells (PAPC). The multilineage differentiation potential suggested some level of cellular plasticity, which these cells share with other stem or progenitor cells. In this context, we have shown that PAPCs indeed express neural stem cell and markers for developing neurons in the brain and that PAPCs morphologically mature into neurons over time. The stem/progenitor properties of PAPCs raises the hope that they might be valuable for studying the functional integration of foreign cells into preexisting tissues and organs, for example in cellular therapies. The functional integration of transplanted cells and their connectivity to the host circuitry is still a major bottleneck in cellular therapies particularly for the brain. The animal models of fetomaternal microchimerism might provide valuable insights into the mechanism how cells survive, migrate, integrate and differentiate in a foreign environment of a host. This review discusses some of the recent findings in the field of fetomaternal microchimerism. It also tries to identify some major gaps of knowledge and raises some questions resulting from the recent advances. Studying fetomaternal microchimerism and the properties of PAPCs in greater detail might pave the way to advance cell based regenerative medicine as well as transplantation medicine.

摘要

孕期胎儿细胞向母体的转移及其器官特异性整合是胎盘脊椎动物中一种广为人知的现象。最近,有报道称在母体中发现的一些胎儿细胞具有祖细胞样特征,如多谱系分化潜能,因此它们被称为妊娠相关祖细胞(PAPC)。多谱系分化潜能表明这些细胞具有一定程度的细胞可塑性,这是它们与其他干细胞或祖细胞共有的特性。在这种情况下,我们已经表明,PAPC确实表达神经干细胞和大脑中发育神经元的标志物,并且随着时间的推移,PAPC在形态上会成熟为神经元。PAPC的干/祖细胞特性带来了一种希望,即它们可能对研究外来细胞在现有组织和器官中的功能整合具有重要价值,例如在细胞治疗中。移植细胞的功能整合及其与宿主回路的连接仍然是细胞治疗尤其是脑部细胞治疗的一个主要瓶颈。母胎微嵌合体的动物模型可能会为细胞在宿主的外来环境中如何存活、迁移、整合和分化的机制提供有价值的见解。这篇综述讨论了母胎微嵌合体领域的一些最新发现。它还试图找出一些主要的知识空白,并提出一些由近期进展引发的问题。更详细地研究母胎微嵌合体和PAPC的特性可能为推进基于细胞的再生医学以及移植医学铺平道路。